Medical Forum / Diseases and Disorders / Alzheimer's / August 2004
Selling a living will to mom.
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Nancy H. - 13 Aug 2004 17:45 GMT My mom read an article suggesting that witholding feeding tubes -- as specified in 'living wills' could cause pain. When you are brain dead, do you feel pain?
I am happy to find this group. I'm caring for my 90 year old mom who thinks she is 100%, but actually has short-term memory loss and repeats herself constantly. Drive me nuts, I expect I'll be back here for help.
Thanks in advance.
Nancy H.
Evelyn Ruut - 13 Aug 2004 18:06 GMT > My mom read an article suggesting that witholding feeding tubes -- as > specified in 'living wills' could cause pain. When you are brain dead, [quoted text clipped - 8 lines] > > Nancy H. If your brain is dead, having someone shove a tube down your throat to keep you alive with some concoction pumping into your stomach, I would imagine that to be a far worse pain for both self and loved ones, than the alternative, a gentler more natural passing. If your brain is dead, what is the purpose of keeping the body alive?
Everyone will eventually have to die, even you and me, and everything that is born eventually dies. Shouldn't it be as natural and as painless as possible. I have a living will and I expressly have forbidden feeding tubes etc.
Pain medications I absolutely would NOT forbid, even though it may shorten the length of ones life. There is no reason I can think of to go out in that much pain, or to prolong the agony by denying pain meds.
Your own values or religious beliefs may vary from that of course, but most people don't want to prolong life artificially with a feeding tube when the mind is so far gone they cannot even eat anymore.
The purpose of life is to experience and to give as much peace and comfort and joy as we can in it. When all of that is totally gone never to return, it would be CRUEL to continue with a feeding tube. Just my humble opinion.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Gwen Love - 13 Aug 2004 19:01 GMT Evelyn, I agree with you 100%. Gwen
> > My mom read an article suggesting that witholding feeding tubes -- as > > specified in 'living wills' could cause pain. When you are brain dead, [quoted text clipped - 31 lines] > and joy as we can in it. When all of that is totally gone never to return, > it would be CRUEL to continue with a feeding tube. Just my humble opinion. Nancy H. - 14 Aug 2004 01:08 GMT Beautifully put, Evelyn! I have printed out a copy for Mom to study (she gets hostile in verbal discussions...)
...
> > When you are brain dead, do you feel pain? > > Nancy H. ...
> If your brain is dead, having someone shove a tube down your throat to keep > you alive with some concoction pumping into your stomach, I would imagine > that to be a far worse pain for both self and loved ones, than the > alternative, a gentler more natural passing. If your brain is dead, what > is the purpose of keeping the body alive? ...
> The purpose of life is to experience and to give as much peace and comfort > and joy as we can in it. When all of that is totally gone never to return, > it would be CRUEL to continue with a feeding tube. Just my humble opinion. Dennis White - 13 Aug 2004 21:56 GMT > My mom read an article suggesting that witholding feeding tubes -- as > specified in 'living wills' could cause pain. When you are brain dead, [quoted text clipped - 8 lines] > > Nancy H. Both my mother and my younger sister had to have "feeding tubes". Both were conscious at the time, and the tubes were inserted directly into their stomachs rather than down their throats. I am no expert on the matter, but I had always believed that it was only breathing tubes that were intubated in the throat. Nutrition is supplied intravenously, and directly to the stomach. I cannot imagine a conscious person having to have food delivered by a tube in the throat. In any case, I would also think that withholding food from an unconscious person would *not* cause pain. This is certainly a question for your mom's doctor. At her age and in her condition, I would hope she has a geriatric specialist. If not, please make plans to visit one right away. Also keep in mind that any condition (withholding or permitting feeding) is up to her. A living will does not designate one way another until it is decided upon by the individual. She should do it now before she is totally incompetent. BTW, legal competence is defined much more broadly than we would apply the term socially and medically.
Dennis White
Darryl - 13 Aug 2004 22:24 GMT >My mom read an article suggesting that witholding feeding tubes -- as >specified in 'living wills' could cause pain.
>When you are brain dead, do you feel pain? Presumably not. This was one of the considerations I made when my 59 y.o. Dad was on his final exit. Probably one of the most painful decisions I've made in my life. In the final days, there are several levels of care--I opted for 'comfort' which was simply fluid for hydration (a glucose drip) (we didn't have a living will but I held medical power of attorney). To this date, I'm convinced that this 'comfort' measure addressed *my* needs.
>I am happy to find this group. They're the greatest group of people that I've never met.
Darryl.
Dennis White - 14 Aug 2004 00:33 GMT > >My mom read an article suggesting that witholding feeding tubes -- as > >specified in 'living wills' could cause pain. [quoted text clipped - 14 lines] > > Darryl. Darryl and everyone else, As caregivers and having tried to second-guess what others may want should convince every single one of us of the need for a living will. There can't be anything more stifling than leaving a loved-one with a difficult moral, ethical or personal decision in a time of crisis! Living wills are not expensive, they save your heirs from probate, they provide for your wishes should you become unable to make your wishes known both while living and after death, and they are solid legal instruments. We should all have them. Take care of it now, even though you believe yourself too young or too healthy to worry about such a thing. You could be hit by a drunk driver later today and either die or left to live out your life in a vegetative state.
Dennis White
Gwen Love - 14 Aug 2004 01:33 GMT How can a "living will" (which applies to health care) keep you out of probate? I think that would require a "trust". Gwen
> > >My mom read an article suggesting that witholding feeding tubes -- as > > >specified in 'living wills' could cause pain. [quoted text clipped - 29 lines] > > Dennis White Dennis White - 14 Aug 2004 03:07 GMT > How can a "living will" (which applies to health care) keep you out of > probate? I think that would require a > "trust". > Gwen You're absolutely right. Many times a "living will" and "revokable living trust" are interchangable names. Usually the part you are recognizing is known as an "advance health directive". It is almost always a part of a revokable living trust. Many people (including me) often use (misuse) the term "living will"to include the entire documents that make up a trust. Revokable trusts also name Durable Powers of Attorney and (at least in the State of Washington, and probably many others) directives affecting mental health care, which is another reason to have the "trust". You may not die, and you may not become vegetative, but what might happen to you if you found yourself permanently brain-damaged? Would you want to be institutionalized? Would you want any or no psychiatric medications, etc?
> > > >My mom read an article suggesting that witholding feeding tubes -- as > > > >specified in 'living wills' could cause pain. [quoted text clipped - 32 lines] > > > > Dennis White Dennis P. Harris - 14 Aug 2004 08:15 GMT > Many times a "living will" and "revokable > living trust" are interchangable names. not in states that have passed a statutory living will law. alaska is one.
AS 18.12 at http://www.legis.state.ak.us/cgi-bin/folioisa.dll/stattx03/query=*/doc/%7Bt7607%7D?
many states have other advance directives defined as statutory powers of attorney: AS 13.26.332-335
http://www.legis.state.ak.us/cgi-bin/folioisa.dll/stattx03/query=*/toc/%7B@81%7D?next
Dennis White - 14 Aug 2004 13:40 GMT > > Many times a "living will" and "revokable > > living trust" are interchangable names. I should have said "many times people use the names "living will" and "revokable living trust" interchangeably. I admit it is incorrect usage.
> not in states that have passed a statutory living will law. > alaska is one. > > AS 18.12 at http://www.legis.state.ak.us/cgi-bin/folioisa.dll/stattx03/query=*/doc/%7Bt7607%7D?
> many states have other advance directives defined as statutory > powers of attorney: AS 13.26.332-335 http://www.legis.state.ak.us/cgi-bin/folioisa.dll/stattx03/query=*/toc/%7B@81%7D?next
I'm not very good at locating specifics in state codesor deciphering their finer points, Does AS 13.26...provide for the individual (rather than an agent, guardian or conservator) to make advance decisions for their own medical care? I think that is the gist of what is known as an Advance Medical Directive (or "living will") commonly in use here in the State of Washington.
Dennis
Dennis P. Harris - 15 Aug 2004 08:57 GMT > I'm not very good at locating specifics in state codesor deciphering their > finer points, Does AS 13.26...provide for the individual (rather than an > agent, guardian or conservator) to make advance decisions for their own > medical care? I think that is the gist of what is known as an Advance > Medical Directive (or "living will") commonly in use here in the State of > Washington. no, that's AS 18.12, which includes the actual form and language. AS 13.26 does the same for durable powers of attorney --- it allows someone to point someone to act on their behalf if they are incapacitated, and provides standards for determining incapacitation.
Nancy H. - 14 Aug 2004 22:59 GMT Thank you for all of your responses. They were very comforting to me but unfortunately my mother misinterpreted my motives and thought I was calling her brain dead to a bunch of strangers. It is disconcerting when I try to ease her mind and wind up being the enemy in her eyes. Her mind is changing and she doesn't realise it. Anyone else have this problem as a caregiver? Nancy H.
Evelyn Ruut - 15 Aug 2004 00:07 GMT > Thank you for all of your responses. They were very comforting to me > but unfortunately my mother misinterpreted my motives and thought I > was calling her brain dead to a bunch of strangers. It is > disconcerting when I try to ease her mind and wind up being the enemy > in her eyes. Her mind is changing and she doesn't realise it. Anyone > else have this problem as a caregiver? Nancy H. Nancy,
It is just another example of how her "reasoner" is broken. I long ago gave up trying to explain her illness to my mother in law.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Tumbleweed - 15 Aug 2004 09:00 GMT > Thank you for all of your responses. They were very comforting to me > but unfortunately my mother misinterpreted my motives and thought I > was calling her brain dead to a bunch of strangers. It is > disconcerting when I try to ease her mind and wind up being the enemy > in her eyes. Her mind is changing and she doesn't realise it. Anyone > else have this problem as a caregiver? Yes, that would be everyone here :-)
 Signature Tumbleweed
email replies not necessary but to contact use; tumbleweednews at hotmail dot com
Songbird - 16 Aug 2004 01:23 GMT > Thank you for all of your responses. They were very comforting to me > but unfortunately my mother misinterpreted my motives and thought I > was calling her brain dead to a bunch of strangers. One of the reasons this NG is never mentioned to my parents! I just tell them I've been "doing some reading on the internet about this kind of stuff, and a lot of the experts seem to recommend..." After all, you folks are experts with a capital E!
Songbird
Evelyn Ruut - 16 Aug 2004 01:48 GMT > > NO_SPAM_TO_dpharris@gci.net (Dennis P. Harris) wrote in message > news:<gfcrh05pchnnhq8len2k0u37gdbl2kgu3g@4ax.com>... [quoted text clipped - 9 lines] > > Songbird I think that part of the what makes this newsgroup special is that there is privacy to some degree, as well as a reasonably immediate feedback for our questions. We can ask even WHILE we are caregiving, without offending our loved ones.
I think many of them might feel offended to think we are "talking about" them. But without that kind of sharing or honesty, how can we ever learn what to do?
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
lynn - 14 Aug 2004 11:34 GMT >(very snipped) > > They're the greatest group of people that I've never met. > > Darryl. Darryl, I agree- and your participation in the group is just one of the many reasons I refer people here all the time! Your kindness and compassion shows through all the time--but your knowledge and scientific mind is a huge bonus for all of us. Thanks for taking the time to be so active here! Lynn
Darryl - 14 Aug 2004 14:23 GMT >>(very snipped) >> [quoted text clipped - 7 lines] >scientific mind is a huge bonus for all of us. Thanks for taking the >time to be so active here! Lynn And thank you for the kind words, Lynn. :-)
Evelyn Ruut - 14 Aug 2004 14:50 GMT > >>(very snipped) > >> [quoted text clipped - 9 lines] > > And thank you for the kind words, Lynn. :-) Darryl, you have helped me personally so many times that I cannot begin to thank you enough for your presence on this newsgroup. But here's a big THANKS anyway!
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Mary Gordon - 14 Aug 2004 17:11 GMT The question of feeding tubes is a complicated one, since all of us have an emotional reaction to the idea of "letting someone starve". We think a feeding tube will help our loved one, keep them healthier and alive longer, let them be more comfortable etc.
When you stand back - there is quite a body of research that suggests that feeding tubes accomplish none of these things for people in late dementia.
Research strongly suggests that tube feeding in patients with late-stage dementia results in: Either no change or an increase in the rate of aspiration and pneumonia (and this is even true of the PEG tubes) No improvement in survival Little or no improvement in weight loss or other nutritional parameters. No reduction in the incidence of pressure sores, and little or no effect on healing of established sores. An increase in the use of physical and chemical restraints Major and minor complications, such as tube obstruction and dislodgment, local and systemic infection, bowel perforation, and death
So.... when a procedure has no benefits or is harmful, I think most of us would wonder ethically why it you'd even go there - I can't see any positives in it. I can see contemplating a tube if the person was in early dementia with good quality of life, and would only need a tube temporarily (i.e. had some temporary illness, and would recover and not need a tube after a short while). Thats just not true of later stage AD.
We elected not to go for tubes and IVs with my MIL, and as I've related here before, she did not seem to be suffering at all. I expect its just part of the natural process of dying - she did not seem to be at all hungry or thirsty, and she gradually ate and drank less and less until she stopped entirely, despite lots of prompting and encouragement, and being offered it many, many times a day. She just had no interest - or maybe she didn't even have enough conscious thought left to interpret physical feelings or know what food or drink was.
We kept her very comfortable. She was not in any pain. She just sort of slowly and peacefully slid away over a period of a couple of weeks. Now, it is hard to watch and do nothing, since particularly in western culture, we have such a hard time coping with death, and accepting that its part of life and inevitable and not always a Bad Thing. We get in our heads that we should fight it to the end, and always be DOING something, rather than sitting quietly, holding their hand, and letting the tide go quietly out. Fighting death in a person with end stage AD is more about our own fears and guilt than it is about what is kindest and most loving for the person who's dying. I mean, we've all seen it - elderly sick loved ones for whom there is no chance of meaningful recovery, and instead of their last days being quiet and loving, they are in some horrible impersonal hospital room and surrounded by a lot of fuss and strangers, being poked and prodded and given a lot of treatment that only makes them uncomfortable and can't hope to do more than give them a few more days of distress.
We went for palliative care only in those last months for my MIL, and that included no treatment of any illness she could have developed beyond comfort measures (i.e. if she'd gotten cancer, or pneumonia or a heart attack, we would not have allowed them to start messing around with her).
Mary G.
Mare - 17 Aug 2004 01:08 GMT Hey Mary, Can you give me some pointers to tell my siblings about palliative care only. They understand not treating cancer and heart attacks but we recently had a pneumonia scare and they wanted it treated. It was a wet cough and scared the c#@$ out of me. Mom had a chest x-ray and it showed no pneumonia but she also had another swallowing eval and she's aspirating food and perhaps saliva so it's really just a matter of time. Of course I've been saying that for a few years now................. My sibs want me to make decisions 99% of the time and I can usually explain things fairly well but this one has me stumped. Yes there is a certain degree of denial going on even after 12 years...sigh. I also don't have any POA's since Mom was in early stages when my dad passed and she blamed me for all sorts of things, so the sibs least likely to do anything have them. They do listen to me most times tho so any helpful explanations would be appreciated.
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> The question of feeding tubes is a complicated one, since all of us > have an emotional reaction to the idea of "letting someone starve". We [quoted text clipped - 13 lines] > parameters. > . No reduction in the incidence of pressure sores, and little or no
> effect on healing of established sores. > . An increase in the use of physical and chemical restraints [quoted text clipped - 44 lines] > > Mary G. Dennis P. Harris - 17 Aug 2004 06:07 GMT > Can you give me some pointers to tell my siblings about > palliative care only. They understand not treating cancer and > heart attacks but we recently had a pneumonia scare and they > wanted it treated. the best source of information in this area is your local hospice organization. they should have brochures, pamphlets, and even books about these kinds of topics. they can also provide counseling for you and other family members regarding end of life decisions.
they should be in your local phone book.
Mare - 20 Aug 2004 02:46 GMT Hey Dennis, Thanks, sometimes it's hard to see the forest thru the trees.
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> > Can you give me some pointers to tell my siblings about > > palliative care only. They understand not treating cancer and [quoted text clipped - 8 lines] > > they should be in your local phone book. lynn - 17 Aug 2004 11:37 GMT (very snipped)
> Hey Mary, > Can you give me some pointers to tell my siblings about > palliative care only. Hi Mare, Dennis is right, hospice can be invaluable as you get closer to the end for mom. Like you, I had no POA, my middle brother did--but yet, I, too, made most of the decisions in her day-to-day care at the NH. When my mom was in her last few months of life, my brother started talking of "having to move her when she needed feeding tubes"--up until then we had been on the same page about things, or so I thought. My oldest brother convinced him to explore the hospice info available on line, and in short order, he agreed to a hospice evaluation--thank goodness! We were then able to allow our beloved mom to die with dignity. As hard as it was to let her to slip away from us, it was the right thing to do for her. (BTW, I had a friend whose dad passed away in late stage Pick's--after a bad pnemonia, it was decided to let hospice provide pallitive care only. They, too, have no regrets) Regards to another "old-timer" on the NG! Lynn
Mare - 20 Aug 2004 02:46 GMT Hey Lynn, Good to see you still around! I think I was just shocked at their reactions. Mom's not on hospice anymore and nothing has really changed since she "graduated" last winter. But I'll look at the info and see what might help the sibs. Thanks
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> (very snipped) > > Hey Mary, [quoted text clipped - 15 lines] > hospice provide pallitive care only. They, too, have no regrets) > Regards to another "old-timer" on the NG! Lynn lynn - 17 Aug 2004 11:38 GMT (very snipped)
> Hey Mary, > Can you give me some pointers to tell my siblings about > palliative care only. Hi Mare, Dennis is right, hospice can be invaluable as you get closer to the end for mom. Like you, I had no POA, my middle brother did--but yet, I, too, made most of the decisions in her day-to-day care at the NH. When my mom was in her last few months of life, my brother started talking of "having to move her when she needed feeding tubes"--up until then we had been on the same page about things, or so I thought. My oldest brother convinced him to explore the hospice info available on line, and in short order, he agreed to a hospice evaluation--thank goodness! We were then able to allow our beloved mom to die with dignity. As hard as it was to let her to slip away from us, it was the right thing to do for her. (BTW, I had a friend whose dad passed away in late stage Pick's--after a bad pnemonia, it was decided to let hospice provide pallitive care only. They, too, have no regrets) Regards to another "old-timer" on the NG! Lynn
turkey in the straw - 18 Aug 2004 04:25 GMT Well,my mom has been home from the hospital a week now.She's been diagnosed with type 2 diabetis.Also we now have to puree all her food and thicken her liquids.I am getting a routine down but its a lot of work.Also i prick her finger 4 times a day.She's gained a lot of her strenghth back too. My family has decided to pay me.Can you believe it????? We are waiting for the closing on the place first though which will be in Nov.Moving up by my sister for help and support.She was down here while my mom was in the hospital and a few days after she came home .I think she seen what a job it all is finally.So thank God for that.Barb
Evelyn Ruut - 18 Aug 2004 12:45 GMT > Well,my mom has been home from the hospital a week now.She's been > diagnosed with type [quoted text clipped - 6 lines] > my mom was in the hospital and a few days after she came home .I think > she seen what a job it all is finally.So thank God for that.Barb Barb, I am so glad to hear that. This is a difficult enough job, with pay. Without it would be a lot worse.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Mare - 18 Aug 2004 15:13 GMT Barb, I'm really glad things have turned around so dramatically for you.
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> Well,my mom has been home from the hospital a week now.She's been > diagnosed with type [quoted text clipped - 6 lines] > my mom was in the hospital and a few days after she came home .I think > she seen what a job it all is finally.So thank God for that.Barb Lee - 18 Aug 2004 19:39 GMT Guess that's what she needed... to see what a job it is.
I'm not paid for caregiving...but also not paying my own way ... partner covers my expenses and so on ... and even, lately, some of my kids' .... partly because I don't have the flexibility to go out and earn my own $$ (because I'm needed here) and partly because its' been MY kids that have pitched in and helped take care of ma for the summer... particularly my oldest, who was here for 5 weeks mamasitting
today, when I was packing up everything I needed so that I could come work from home because there was no one else to be here for ma, he suggested that a) we set up a work area for me here so that it's not such an ordeal to move everything....and b) that he and his sibs need to talk about the whole payment thing, i.e. to set a value on what I do and make sure that it is being recognized and that I'm being paid enough.
It wasn't a particular concern for me... but the fact that he thought of it is awfully nice, I think. The work area will happen ... this week, I think... just have to go out and get another monitor or two, really .... can carry my tools between locations... the rest we'll see about.
> Well,my mom has been home from the hospital a week now.She's been > diagnosed with type [quoted text clipped - 6 lines] > my mom was in the hospital and a few days after she came home .I think > she seen what a job it all is finally.So thank God for that.Barb turkey in the straw - 19 Aug 2004 04:45 GMT I just wish ALL my family felt i should be pd.But,who cares!!!!! When ya think about it we all do the jobs of many people.At least 5 different people came into my moms room every day.Now i do it all. Going to my sisters again for a few days.I got to go to the casino last time.It was awesome.Going again this time.My mom loves to watch the deer that they feed in there yard.We seen 6 at once last time. Do any of you have to test blood sugars?Or puree foods?Boy thickened water is icky.Other than water my mom just thinks its a slushy.LOL I am sooo surprised she is doing so good with this new way of eating.Well,have a great evening.Barb
Mare - 20 Aug 2004 02:48 GMT Hi Barb, When Mom was at home I did test her sugar twice a day. She was well controlled after we hid the food;~) I did learn(not sure it's still acceptable) that older folks with dementia shouldn't be held to the same numbers as the rest of us. We kept Mom between 120 and 140. Be careful of really low sugars since they can really screw up a person with dementia.
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> I just wish ALL my family felt i should be pd.But,who cares!!!!! When ya > think about it we all do the jobs of many people.At least 5 different [quoted text clipped - 6 lines] > slushy.LOL I am sooo surprised she is doing so good with this new way of > eating.Well,have a great evening.Barb Songbird - 20 Aug 2004 20:45 GMT > Hi Barb, > When Mom was at home I did test her sugar twice a day. She was [quoted text clipped - 3 lines] > between 120 and 140. Be careful of really low sugars since they > can really screw up a person with dementia. Did you test fasting or after meals? Doc has my dad testing post-meals right now and his LOWEST has been 214. (and he's on medication!)
Songbird
Evelyn Ruut - 20 Aug 2004 23:50 GMT > > Hi Barb, > > When Mom was at home I did test her sugar twice a day. She was [quoted text clipped - 7 lines] > > Songbird One should test both fasting AND after meals, both the 1 hour and 2 hour afterwards.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Songbird - 21 Aug 2004 00:06 GMT > One should test both fasting AND after meals, both the 1 hour and 2 hour > afterwards. It'll never happen -- he's already complaining that all his fingertips are bruised with testing twice a day. We tried taking blood from the forearm, and that didn't work. Tough skin, I guess.
Songbird
Evelyn Ruut - 21 Aug 2004 01:10 GMT > > One should test both fasting AND after meals, both the 1 hour and 2 hour > > afterwards. [quoted text clipped - 3 lines] > > Songbird Songbird, it is important to stick the finger on the side rather than on the pads. Hurts less. I am speaking of the first phalange like where the fingerprints are, but on the side, not the actual pad.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Mare - 21 Aug 2004 02:32 GMT Songbird, Evelyn is right. He needs to test more often til he can identify what foods spike his blood sugar and then modify what he eats. He might even need more or different meds. When first starting to control diabetes he also needs to figure out what meds help him. Maybe you should subscribe to the diabetes newsgroup to learn more. It's been a few years since I subscribed but there was very helpful info to be found. Oh, back then they also had lots of blow ups so just ignore those if you can. You know with the 214 that could definitely be affecting his mental status and control could restore some abilities.
 Signature Mare mfcoleman@THEOLEmindspring.com http://www.muggsmulcher.com/kstuff/a.s.a/intro.htm alt.support.alzheimers' FAQs and Stuff Pages
> > Hi Barb, > > When Mom was at home I did test her sugar twice a day. She was [quoted text clipped - 7 lines] > > Songbird turkey in the straw - 26 Aug 2004 05:42 GMT Songbird, We test before meals.Tonight my moms was 77.But it has been as high as 287.My moms jumps all over the place.It hard to get it leveled out.Barb
Evelyn Ruut - 26 Aug 2004 12:57 GMT > Songbird, > We test before meals.Tonight my moms was 77.But it has been as high > as 287.My moms jumps all over the place.It hard to get it leveled > out.Barb That is shockingly high. Are you limiting carbohydrates?
You should be if her BG's are that high. That is organ damaging territory.
I would limit bread, potatoes, pasta and white rice severely if I were you, and try to make her fill up on salad, lower carb vegetables, and protein instead.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
turkey in the straw - 27 Aug 2004 04:09 GMT Evelyn, My mom has not had bread in weeks.We are just new at this and learning every day.I have limited carbs very much.But they fed her much more carbs in the hospital than i do.One thing i noticed is today her BS was vey good and she was so much more awake all day.High BS really drains them.Barb
Evelyn Ruut - 27 Aug 2004 12:49 GMT > Evelyn, > My mom has not had bread in weeks.We are just new at this and > learning every day.I have limited carbs very much.But they fed her much > more carbs in the hospital than i do.One thing i noticed is today her BS > was vey good and she was so much more awake all day.High BS really > drains them.Barb Hi Barb,
It sure does. Totally exhausting.
You might want to try the newsgroup alt.support.diabetes, as they have a lot of good advice to offer.
 Signature Regards, Evelyn
(to reply to me personally, remove 'sox")
Robert E. Lewis - 27 Aug 2004 23:40 GMT > Evelyn, > My mom has not had bread in weeks.We are just new at this and > learning every day.I have limited carbs very much.But they fed her much > more carbs in the hospital than i do.One thing i noticed is today her BS > was vey good and she was so much more awake all day.High BS really > drains them.Barb Yeah... I find high BS levels really wear me out, too....
I bet high blood sugar can have an effect, too.
<G>
 Signature Robert
turkey in the straw - 28 Aug 2004 04:54 GMT Robert, That was cute!!!! Barb
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